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  2. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    The latter reaction is also viable laboratory synthesis. One laboratory technique for substitutive bromination treats propanol with a mixture of hydrobromic and sulfuric acids: CH 3 CH 2 CH 2 OH + HBr → CH 3 CH 2 CH 2 Br + H 2 O. Alternate synthetic routes include treating propanol with phosphorus tribromide [4] or via a Hunsdiecker reaction ...

  3. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    It is used in the synthesis of several common aroma compounds (cyclamen aldehyde, helional, lilial). [2] Reduction of propionaldehyde gives n‑propanol, and reductive amination gives propanamine. Rising demand for non-chlorocarbon solvents has caused some manufacturers to substitutively brominate n‑propanol to propyl bromide.

  4. Myers allene synthesis - Wikipedia

    en.wikipedia.org/wiki/Myers_allene_synthesis

    In organic chemistry, the Myers allene synthesis is a chemical reaction that converts a propargyl alcohol into an allene by way of an arenesulfonyl hydrazine as a key intermediate. [1] This name reaction is one of two discovered by Andrew Myers that are named after him; both this reaction and the Myers deoxygenation reaction involve the same ...

  5. Crabbé reaction - Wikipedia

    en.wikipedia.org/wiki/Crabbé_reaction

    In broad strokes, the mechanism of the reaction is believed to first involve a Mannich-like addition of the alkynylmetal species into the iminium ion formed by condensation of the aldehyde and the secondary amine. This first part of the process is a so-called A 3 coupling reaction (A 3 stands for aldehyde-alkyne-amine).

  6. Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Mannich_reaction

    In organic chemistry, the Mannich reaction is a three-component organic reaction that involves the amino alkylation of an acidic proton next to a carbonyl (C=O) functional group by formaldehyde (H−CHO) and a primary or secondary amine (−NH 2) or ammonia (NH 3). [1]

  7. Hydroformylation - Wikipedia

    en.wikipedia.org/wiki/Hydroformylation

    In organic chemistry, hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes (R−CH=O) from alkenes (R 2 C=CR 2). [ 1 ] [ 2 ] This chemical reaction entails the net addition of a formyl group ( −CHO ) and a hydrogen atom to a carbon-carbon double bond .

  8. Organic synthesis - Wikipedia

    en.wikipedia.org/wiki/Organic_synthesis

    Before beginning any organic synthesis, it is important to understand the chemical reactions, reagents, and conditions required in each step to guarantee successful product formation. When determining optimal reaction conditions for a given synthesis, the goal is to produce an adequate yield of pure product with as few steps as possible. [13]

  9. Aldol reaction - Wikipedia

    en.wikipedia.org/wiki/Aldol_reaction

    Aldol structural units are found in many important molecules, whether naturally occurring or synthetic. [8] [9] The reaction is well used on an industrial scale, notably of pentaerythritol, [10] trimethylolpropane, the plasticizer precursor 2-ethylhexanol, and the drug Lipitor (atorvastatin, calcium salt). [11]